BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUNBEAM

    MDR report key: 1367012 · Received February 9, 2009

    Report

    Report Number
    1043899-2009-00013
    Event Type
    Malfunction
    Date Received
    February 9, 2009
    Report Date
    February 9, 2009
    Manufacturer
    JARDEN CONSUMER SOLUTIONS, DBA, SUNBEAM PRODUCTS
    Product Code
    KFZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    .

    Description of Event or Problem · 1

    THE CONSUMER REPORTED THE VAPORIZER OVERHEATED AND MELTED A HOLE IN THE TOP OF THE UNIT. NO INJURIES WERE REPORTED WITH THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUNBEAM VAPORIZER KFZ JARDEN CONSUMER SOLUTIONS, DBA, SUNBEAM PRODUCTS 1387 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Other